MAUDE Adverse Event Report: BAUSCH + LOMB ENVISTA INTRAOCULAR LENS PRELOADED

Model Number	MX60PL
Medical Device Problem Code	Crack (1135)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/19/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The device was discarded and not returned for evaluation.A review of the device history record (dhr) did not find any non-conformities or anomalies related to the reported event.The trend analysis, risk analysis, and directions for use are considered acceptable with the product performing within anticipated rates.Corrective measures have been identified to mitigate future similar occurrences.Bausch & lomb will continue to monitor similar events to determine if additional actions are required.
Event or Problem Description
It was reported that during implantation of an intraocular lens (iol) into the right eye, the surgeon noticed an approximately 4mm crack in the lens optic starting near the optic/haptic junction and extending towards the center of the lens.The iol was removed from the eye and a successful intraoperative lens exchange was performed using a backup iol of the same model and diopter.A suture was placed across the main incision to close the wound.In the surgeon's opinion, the most likely cause of event is the defective lens.Patient prognosis is stable.

• Brand Name: ENVISTA INTRAOCULAR LENS PRELOADED
• Common Device Name: INTRAOCULAR LENS
• Manufacturer (Section D): BAUSCH + LOMB; 1400 north goodman street; rochester NY 14609
• Manufacturer (Section G): BAUSCH + LOMB; 21 n park pl blvd; clearwater FL 33759
• Manufacturer Contact: shayan habibi ; 21 north park place blvd.; clearwater, FL 33759 ; 7277246600
• MDR Report Key: 21118329
• Report Number: 0001313525-2025-00002
• Device Sequence Number: 8683065
• Product Code: HQL
• UDI-Device Identifier: 10757770571274
• UDI-Public: (01)10757770571274(17)260731
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: P910056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 12/10/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 07/31/2026
• Device Model Number: MX60PL
• Device Catalogue Number: MXUEPL0700
• Device Lot Number: 3P20839
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/10/2024
• Initial Report FDA Received Date: 01/09/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 08/07/2023
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: SIMPLIFEYE INSERTER FOR ENVISTA
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 49 YR
• Patient Sex: Unknown